Canonical Allele Identifier: CA13431655
Gene: HSPA8 HGNC NCBI
SNORD14D HGNC NCBI

Linked Data

dbSNP Id: rs1461496

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123058916A>G , CM000673.2:g.123058916A>G GRCh38
NC_000011.9:g.122929624A>G , CM000673.1:g.122929624A>G GRCh37
NC_000011.8:g.122434834A>G NCBI36
NG_029473.1:g.8221T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000534624.6:c.1324-86T>C (HSPA8) MANE Select ENSP00000432083.1:n.1324-86T>C
ENST00000227378.7:c.1324-86T>C (HSPA8) ENSP00000227378.3:n.1324-86T>C
ENST00000453788.6:c.1324-86T>C (HSPA8) ENSP00000404372.2:n.1324-86T>C
ENST00000524552.5:c.97-86T>C (HSPA8) ENSP00000435908.1:n.97-86T>C
ENST00000526110.5:c.1267-86T>C (HSPA8) ENSP00000433584.1:n.1267-86T>C
ENST00000526686.1:c.-107T>C (HSPA8) ENSP00000435019.1:n.-107T>C
ENST00000532091.1:n.1213T>C (HSPA8)
ENST00000532636.5:c.1324-86T>C (HSPA8) ENSP00000437125.1:n.1324-86T>C
ENST00000533238.5:n.426-86T>C (HSPA8)
ENST00000533540.5:c.886-86T>C (HSPA8) ENSP00000437189.1:n.886-86T>C
ENST00000534319.5:c.616-86T>C (HSPA8) ENSP00000433316.1:n.616-86T>C
ENST00000534624.5:c.1324-86T>C (HSPA8) ENSP00000432083.1:n.1324-86T>C
NM_006597.5:c.1324-86T>C (HSPA8) NP_006588.1:n.1324-86T>C
NM_153201.3:c.1324-86T>C (HSPA8) NP_694881.1:n.1324-86T>C
NR_001454.2:n.80T>C (SNORD14D)
XM_011542798.1:c.1324-86T>C (HSPA8) XP_011541100.1:n.1324-86T>C
NM_006597.6:c.1324-86T>C (HSPA8) MANE Select NP_006588.1:n.1324-86T>C
NM_153201.4:c.1324-86T>C (HSPA8) NP_694881.1:n.1324-86T>C